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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380Generated: October 26, 2026

Triisopropyl borate → (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid

https://huagongshe.com/reaction/1380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 10586063—
ReactantButyllithiumHCID 178418339—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
Product(5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acidHCID 22571498—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cold (-78° C.) solution of 2.02 g (8.4 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene in 11.0 mL of toluene, was added 4.6 g (6.8 mL, 10.9 mmol, 1.6M in hexane) of n-BuLi. The resulting solution was stirred at -78° C. for 45 min. and then 2.40 g (3.0 mL, 12.7 mmol) of triisopropylborate was dropwise added and the reaction stirred at room temperature for 12 h. The reaction was then diluted with 10% HCl, and extracted with ether (2×). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Recrystallization from hexane afforded the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723666
Source datasetuspto-grants-1998_03
ORD IDord-1def6f145a124de08c583f52bfc46d3d
Source noteuspto-grants-1998_03